10,000 results
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14ms
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Sources: EU EUDAMED, US FDA
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Status: Terminated
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AXIOM Artis X-ray systems running software versions VB11K and VB22G
FDA Recall
Terminated
·Siemens Medical Solutions USA, Inc·Product code IZI·March 10, 2006
Mavig Portegra 2 which is an accessory to the Siemens angiographic, fluoroscopic and radiographic imaging systems. Component material number 7559375 Upper Body radiation shield, Artis T.
FDA Recall
Terminated
·Siemens Medical Solutions USA, Inc·Product code IZI·May 1, 2009
Koodinat M/MP Patient Table used with Angiostar Model 5294009. The device is used as an Angiographic X-Ray System.
FDA Recall
Terminated
·Siemens Medical Solutions USA, Inc·Product code IZI·July 1, 2009
Shimadzu Digital Radiography X-Ray System, Catalog No. DAR-8000f. This device is intended to be used for radiography in the hospital with X-ray devices.
FDA Recall
Terminated
·Shimadzu Medical Systems·Product code IZI·April 3, 2014
POLYSTAR T.O.P., Angiographic X-Ray System, Model Numbers 1148902 and 4784505.
FDA Recall
Terminated
·Siemens Medical Solutions USA, Inc·Product code IZI·September 23, 2004
POLYSTAR, Angiographic X-Ray System, Model 1148902
FDA Recall
Terminated
·Siemens Medical Solutions USA, Inc·Product code IZI·September 23, 2004
Allura Xper FD10/10 x-ray system
FDA Recall
Terminated
·Philips Medical Systems North America Co. Phillips·Product code IZI·February 6, 2006
FD 10/10 X-Ray System, Angiograph, bi-plane digital Allura FD, 10' detector
FDA Recall
Terminated
·Philips Medical Systems North America Co. Phillips·Product code IZI·December 14, 2006
Monitor Ceiling Suspension for Fluoroscopic and Angiographic X-Ray Systems.
FDA Recall
Terminated
·Philips Medical Systems Sales & Service Region No. America·Product code IZI·October 10, 2003
AXIOM Artis System dFA using software version VB31D with 30x40 cm2 flat detectors. AXIOM Artis is a angiography system developed for single and biplane diagnostic imaging and interventional procedures.
FDA Recall
Terminated
·Siemens Medical Solutions USA, Inc·Product code IZI·August 25, 2008
AXIOM Artis System dTA using software version VB31D with 30x40 cm2 flat detectors. AXIOM Artis is a angiography system developed for single and biplane diagnostic imaging and interventional procedures.
FDA Recall
Terminated
·Siemens Medical Solutions USA, Inc·Product code IZI·August 25, 2008
Axiom Artis Zee. Angiographic X-ray System.
FDA Recall
Terminated
·Siemens Medical Solutions USA, Inc·Product code IZI·August 22, 2008
Bicor X-Ray System, Model number 9023136.
FDA Recall
Terminated
·Siemens Medical Solutions USA, Inc·Product code IZI·August 11, 2008
COROSKOP HS-ACS X-Ray System, Model number 6134659.
FDA Recall
Terminated
·Siemens Medical Solutions USA, Inc·Product code IZI·August 11, 2008
Integris XPER FD10 F/C
FDA Recall
Terminated
·Philips Medical Systems North America Co. Phillips·Product code IZI·December 10, 2008
Allura XPER 10/10
FDA Recall
Terminated
·Philips Medical Systems North America Co. Phillips·Product code IZI·December 10, 2008
MONOPLANE X-ray Imaging Systems include the Allura XPER FD10 F/C, Allura XPER FD20, Integris H5000/Allura 9 F/C, Integris CV, and Allura 12-15 Monoplane. The Monoplane system has one C-arm and it could be mounted on a ceiling or on the floor stand. The product's brochure is labeled in part: "Philips Healthcare Global Information Center...P.O. Box 1286...5602 BG Eindhoven...The Netherlands".
FDA Recall
Terminated
·Philips Medical Systems North America Co. Phillips·Product code IZI·February 4, 2010
BIPLANE X-ray Imaging Systems included Allura XPER FD10/10, FD20/10, FD20/20, Integris BH5000, and Integris Allura 12-15 Biplane. The BIPLANE system has two C-arms and it allows the operator to image in two planes: Lateral and Frontal. It has a C-arm on the stand and C-arm suspended from the ceiling. The product's brochure is labeled in part: "Philips Healthcare Global Information Center...P.O. Box 1286...5602 BG Eindhoven...The Netherlands".
FDA Recall
Terminated
·Philips Medical Systems North America Co. Phillips·Product code IZI·February 4, 2010
Product consists of a syringe used to inject fluids during an angiographic procedure for fluoroscopic imaging. Labeling is as follows: Product Label ''***Argon Medical Device***REORDER NO./REF 193205***10cc Control Syringe FR/TR/FM w/ Reservoir***This device is designed for the administration and removal of fluids***DISPOSABLE***SINGLE USE ONLY***DO NOT RESTERILIZE***STERILE***EO***STERILIZED BY EtO***Sterile Unless Opened or Damaged***Argon Medical Devices, Inc. 1445 FLAT CREEK ROAD - ATHENS, TX 75751***800-927-4669***'' Carton Label ''***Argon Medical Device***10cc Control Syringe FR/TR/FM w/ Reservoir***This device is designed for the administration and removal of fluids***REF/REORDER NO. 193205***Quantity: 25ea***STERILE***EO***STERILIZED BY EtO***DISPOSABLE***SINGLE USE ONLY***DO NOT RESTERILIZE***Sterile Unless Opened or Damaged***Argon Medical Devices, Inc. 1445 FLAT CREEK ROAD - ATHENS, TX 75751***800-927-4669***''
FDA Recall
Terminated
·Argon Medical Devices, Inc·Product code IZI·June 27, 2005
Allura Xper FD 20/10 x-ray, and fluoroscopy
FDA Recall
Terminated
·Philips Medical Systems North America Co. Phillips·Product code IZI·October 12, 2006